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Unraveling Differential Transcriptomes and Cell Types in Zebrafish Larvae Intestine and Liver
The zebrafish intestine and liver, as in other vertebrates, are derived from the endoderm. Great effort has been devoted to deciphering the molecular mechanisms controlling the specification and development of the zebrafish intestine and liver; however, genome-wide comparison of the transcriptomes b...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9600436/ https://www.ncbi.nlm.nih.gov/pubmed/36291156 http://dx.doi.org/10.3390/cells11203290 |
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author | Gao, Yuqi Jin, Qingxia Gao, Ce Chen, Yayue Sun, Zhaoxiang Guo, Guoji Peng, Jinrong |
author_facet | Gao, Yuqi Jin, Qingxia Gao, Ce Chen, Yayue Sun, Zhaoxiang Guo, Guoji Peng, Jinrong |
author_sort | Gao, Yuqi |
collection | PubMed |
description | The zebrafish intestine and liver, as in other vertebrates, are derived from the endoderm. Great effort has been devoted to deciphering the molecular mechanisms controlling the specification and development of the zebrafish intestine and liver; however, genome-wide comparison of the transcriptomes between these two organs at the larval stage remains unexplored. There is a lack of extensive identification of feature genes marking specific cell types in the zebrafish intestine and liver at 5 days post-fertilization, when the larval fish starts food intake. In this report, through RNA sequencing and single-cell RNA sequencing of intestines and livers separately dissected from wild-type zebrafish larvae at 5 days post-fertilization, together with the experimental validation of 47 genes through RNA whole-mount in situ hybridization, we identified not only distinctive transcriptomes for the larval intestine and liver, but also a considerable number of feature genes for marking the intestinal bulb, mid-intestine and hindgut, and for marking hepatocytes and cholangiocytes. Meanwhile, we identified 135 intestine- and 97 liver-enriched transcription factor genes in zebrafish larvae at 5 days post-fertilization. Our findings provide rich molecular and cellular resources for studying cell patterning and specification during the early development of the zebrafish intestine and liver. |
format | Online Article Text |
id | pubmed-9600436 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96004362022-10-27 Unraveling Differential Transcriptomes and Cell Types in Zebrafish Larvae Intestine and Liver Gao, Yuqi Jin, Qingxia Gao, Ce Chen, Yayue Sun, Zhaoxiang Guo, Guoji Peng, Jinrong Cells Article The zebrafish intestine and liver, as in other vertebrates, are derived from the endoderm. Great effort has been devoted to deciphering the molecular mechanisms controlling the specification and development of the zebrafish intestine and liver; however, genome-wide comparison of the transcriptomes between these two organs at the larval stage remains unexplored. There is a lack of extensive identification of feature genes marking specific cell types in the zebrafish intestine and liver at 5 days post-fertilization, when the larval fish starts food intake. In this report, through RNA sequencing and single-cell RNA sequencing of intestines and livers separately dissected from wild-type zebrafish larvae at 5 days post-fertilization, together with the experimental validation of 47 genes through RNA whole-mount in situ hybridization, we identified not only distinctive transcriptomes for the larval intestine and liver, but also a considerable number of feature genes for marking the intestinal bulb, mid-intestine and hindgut, and for marking hepatocytes and cholangiocytes. Meanwhile, we identified 135 intestine- and 97 liver-enriched transcription factor genes in zebrafish larvae at 5 days post-fertilization. Our findings provide rich molecular and cellular resources for studying cell patterning and specification during the early development of the zebrafish intestine and liver. MDPI 2022-10-19 /pmc/articles/PMC9600436/ /pubmed/36291156 http://dx.doi.org/10.3390/cells11203290 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Gao, Yuqi Jin, Qingxia Gao, Ce Chen, Yayue Sun, Zhaoxiang Guo, Guoji Peng, Jinrong Unraveling Differential Transcriptomes and Cell Types in Zebrafish Larvae Intestine and Liver |
title | Unraveling Differential Transcriptomes and Cell Types in Zebrafish Larvae Intestine and Liver |
title_full | Unraveling Differential Transcriptomes and Cell Types in Zebrafish Larvae Intestine and Liver |
title_fullStr | Unraveling Differential Transcriptomes and Cell Types in Zebrafish Larvae Intestine and Liver |
title_full_unstemmed | Unraveling Differential Transcriptomes and Cell Types in Zebrafish Larvae Intestine and Liver |
title_short | Unraveling Differential Transcriptomes and Cell Types in Zebrafish Larvae Intestine and Liver |
title_sort | unraveling differential transcriptomes and cell types in zebrafish larvae intestine and liver |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9600436/ https://www.ncbi.nlm.nih.gov/pubmed/36291156 http://dx.doi.org/10.3390/cells11203290 |
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